Medicines Evaluation Board, Utrecht, the Netherlands; Department of Medical Informatics, Erasmus MC, Rotterdam, the Netherlands.
Department of Medical Informatics, Erasmus MC, Rotterdam, the Netherlands; Médecins Sans Frontières, Amsterdam, the Netherlands.
Vaccine. 2020 Mar 30;38(15):3086-3095. doi: 10.1016/j.vaccine.2020.02.074. Epub 2020 Mar 5.
Serious adverse reactions after immunization are rare but do occur. In very rare instances, cases with fatal outcome have been reported. These reports can have a huge impact and even more so when due to an immunization error. The aim of this study is to systematically review immunization errors with fatal outcomes in EudraVigilance.
This was a case-series analysis of Individual Case Safety Reports (ICSRs) reporting immunization errors and a fatal outcome. To determine the level of certainty of a causal association between the immunization errors and fatal outcomes two independent reviewers assessed all ICSRs using the WHO tool "Causality assessment of an Adverse Event Following Immunization (AEFI)". In accordance with the tool, the ICSRs were classified as consistent, indeterminate, inconsistent/coincidental, or unclassifiable. In addition, we estimated the contribution of reported errors to the fatal outcomes as large, moderate, small, none, or unclassifiable using a classification developed for this study.
A total of 154 ICSRs met the inclusion criteria. Vaccines reported most frequently were pneumococcal (33), rabies (27) and influenza vaccines (24). Most frequently reported errors were non-compliance with recommended schedules of immunization (63). The most frequently reported vaccine-error combination was rabies vaccines and non-compliance with a recommended schedule of immunization (23). Twelve cases were classified as consistent with causal association and had a large error contribution. These cases concerned a cluster of six cases reporting incorrect handling of multi-dose vials containing measles vaccine and six cases reporting administration of live-attenuated vaccines to immunocompromised patients.
In this study, we showed that fatal outcomes following immunization errors are very rare. Four key issues were the importance of: (1) quality control of multi-dose vaccines, (2) screening patients for immunocompromising factors, (3) education on the importance of adherence, and (4) measures to improve distinction between vaccines and medicines.
接种后发生严重不良反应的情况较为罕见,但确实存在。在极少数情况下,已有报告出现致命后果的病例。这些报告可能会产生巨大影响,尤其是由于接种错误而导致的报告。本研究旨在系统地审查 EudraVigilance 中因接种错误而导致致命后果的案例。
这是一项对报告接种错误和致命后果的个别病例安全报告(ICSR)的病例系列分析。为了确定接种错误与致命后果之间因果关系的确定性程度,两名独立审查员使用世界卫生组织(WHO)的工具“疫苗接种后不良事件(AEFI)因果关系评估”评估了所有 ICSR。根据该工具,ICSR 被分类为一致、不确定、不一致/偶合或无法分类。此外,我们使用为此研究开发的分类法,估计报告的错误对致命后果的贡献为大、中、小、无或无法分类。
共有 154 份 ICSR 符合纳入标准。报告最频繁的疫苗是肺炎球菌(33)、狂犬病(27)和流感疫苗(24)。最常报告的错误是未遵守推荐的免疫接种时间表(63)。报告最频繁的疫苗-错误组合是狂犬病疫苗和未遵守推荐的免疫接种时间表(23)。有 12 例被归类为与因果关系一致,且错误贡献较大。这些病例涉及一组六例报告麻疹疫苗多剂量小瓶处理不当和六例报告活减毒疫苗用于免疫功能低下患者的病例。
在本研究中,我们表明接种错误后发生致命后果的情况非常罕见。有四个关键问题需要重视:(1)多剂量疫苗的质量控制,(2)筛选免疫功能低下患者的因素,(3)关于遵守接种要求重要性的教育,以及(4)改善疫苗和药物区分的措施。